Lot numbers can be found on the outside label of a product:
Thianthrene 5-oxide
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CAS No. 2362-50-7
- Cat. No. CS-0135499
- Purity≥96%
- MDL No.None
*For research and further manufacturing use only, not for direct human use.
Structure of 2362-50-7
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General Information
- CAS No. 2362-50-7
- Cat. No. CS-0135499
- Purity ≥96%
- MDL No. None
- Storage 4°C, stored under nitrogen
- Shipping Room temperature in continental US; may vary elsewhere.
- Molecular Formula C₁₂H₈OS₂
- Molecular Weight 232.32
- Synonym(s) 5λ4-Thianthren-5-one
- SMILES O=S1C2=CC=CC=C2SC3=C1C=CC=C3
Application
Thianthrene 5-oxide serves as a reliable sulfur-transfer reagent in synthetic organic chemistry, enabling efficient sulfenylation of nucleophiles under mild conditions. Its bench-stable nature and compatibility with diverse functional groups facilitate practical implementation in complex molecule synthesis. Widely employed in the construction of thioether linkages and sulfur-containing heterocycles, it functions as a selective, high-yielding alternative to traditional sulfuration agents in established reaction workflows.
Synthesis
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Route1
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In-stock
92-85-3 - ~99%
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In-stock
2362-50-7
References
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Bosch, Eric; Kochi, Jay K. Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1995 , # 8 p. 1057 - 1064
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Route2
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35787-71-4 - ~15%
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In-stock
2362-50-7
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In-stock
92-85-3
References
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Ando, Wataru; Kabe, Yoshio; Kobayashi, Shohei; Takyu, Choichi; Yamagishi, Akio; Inaba, Humio Journal of the American Chemical Society, 1980 , vol. 102, # 13 p. 4526 - 4528
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Route3
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60896-34-6 - ~72%
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In-stock
2362-50-7
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In-stock
92-85-3
References
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Boduszek, Bogdan; Shine, Henry J. Journal of Organic Chemistry, 1988 , vol. 53, # 21 p. 5142 - 5143
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Safety Information
Download SDS|
GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H302-H315-H319-H335
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Precautionary Statements : P261-P280-P302+P352
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Quality Control
Computational Chemistry Data
- TPSA 17.07
- LogP 3.3179
- H_Acceptors 2
- H_Donors 0
- Rotatable_Bonds 0
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